Jobs at Cellares

The HR Business Partner serves as the on-site HR resource, providing employee support and managing HR processes in a manufacturing environment while partnering with leadership to ensure compliance and improve HR practices.

Lead a QC team at a GMP cell therapy manufacturing site to manage analytical testing, method development/validation, stability programs, equipment qualification, investigations (OOS), data review, regulatory documentation, and QC quality systems. Interface cross-functionally, support audits, train analysts, manage contract lab transfers, and assist regulatory dossier preparation.

Support MSAT technology transfer and scale-up for cell therapy manufacturing. Drive process automation, ensure GMP readiness, maintain process knowledge and capability through data analysis, lead root cause investigations, CAPA, change control, FMEA, and validation activities. Write SOPs and batch records, define equipment requirements, provide training, and coordinate cross-functional stakeholders.

The Manufacturing Supervisor oversees cGMP operations and manages the production of cell therapy products, ensuring compliance, team development, and process optimization.

The Manufacturing Support Services Specialist supports manufacturing and warehouse operations, performing routine procedures in a GMP environment, training new associates, and ensuring compliance with SOPs and safety policies.

The Senior Director of IDMO Site Quality leads QA/QC operations for cell therapy manufacturing, ensuring compliance with cGMP while fostering collaboration across departments and stakeholders for successful product outcomes.

Cellares seeks a Senior Scientist in Process Development to execute and analyze experiments for cell therapy, interface cross-functionally, and mentor junior staff.

The Automation Engineer will develop and optimize automated QC workflows, troubleshoot systems, and support laboratory operations in a GMP environment.

Design and execute cell therapy process development and scale-up experiments, maintain primary cell lines and leukopaks, draft SOPs and batch documentation, analyze process data, troubleshoot semi-automated instruments and LIMS, and implement corrective actions to advance the Cellares automated cell therapy manufacturing platform.

Design and execute experiments (including DOE) to develop and scale cell therapy processes. Collaborate cross-functionally to transfer technologies, author technical documentation, analyze and present results, train staff, troubleshoot processes, and provide technical feedback to engineering and manufacturing teams.

Lead process development and technology transfer for autologous and allogeneic cell therapies, manage and mentor teams, coordinate cross-functional programs, author technical documentation, and evaluate new technologies to optimize the Cellares manufacturing platform.

Support design and execution of small-scale and scale-up cell therapy process development experiments using the Cellares platform. Perform cell line maintenance, leukopak processing, gene modification, expansion, cryopreservation, equipment qualification, SOP/report authoring, data analysis, and routine lab tasks to advance automated cell therapy manufacturing processes.

Lead and execute stabilization, scaling, and continuous improvement of GMP-critical systems (ERP, MES, QMS, PLM, LIMS, integrations). Act as a hands-on player-coach bridging Manufacturing, Quality, Supply Chain, Engineering, and Finance to ensure data integrity, traceability, audit readiness, and operational execution while governing releases, validations, vendor performance, and cross-system issue resolution.

The Quality Control Analyst will perform analytical testing, including in-process, lot release, and stability testing while ensuring compliance with cGMP guidelines. They will also investigate discrepancies and support equipment validation and documentation for regulatory submissions.

The Director, Operations Finance will oversee FP&A for the Operations organization, driving financial insights, cost forecasts, and operational efficiencies across manufacturing sites globally.

The Automation Engineer will develop and optimize lab automation systems, validate QC workflows, and ensure functionality of automated systems for cell therapy manufacturing.

The Director, Corporate FP&A leads financial planning processes, collaborates with functional leaders, and provides analysis to drive financial performance in a biotechnology setting.

The Senior Electrical Engineer will lead electrical design for automation equipment, ensuring compliance and managing design documentation. Responsibilities include collaborating with teams, conduct prototyping, and driving design reviews based on industry standards.

The Director of Enterprise Programs leads client programs in process development, managing teams, overseeing tech transfer, ensuring compliance, and optimizing manufacturing processes for cell therapies.

Lead and support IT/OT operations in a biotech manufacturing lab, ensuring system reliability and compliance with industry regulations.